# K926203: Endoscopic Scissors (Disposable/Reusable Shafts)

- Pathway: 510(k) (Traditional)
- Applicant: Weck Endoscopy
- Decided: Oct 15, 1993 after 310 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
9 later devices descend from it; 1 cites it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K014207: Reposable Instrument System, Models MF001-MF083 (2002), 8 descendants of its own
- K063485: Logic Laparoscopic Scissors (2006), 7 descendants of its own
- K090583: Endoscopic Monopolar Scissors, Models Ems-235, Ems-165 (2009), 4 descendants of its own
- K141058: Ensizor Endoscopic Scissors (2014), 3 descendants of its own
- K150939: Ensizor Endoscopic Scissors (2015), 2 descendants of its own

Source page: https://510kreport.com/device/K926203
Methodology: https://510kreport.com/methodology